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Showing results (441-450 of 550) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 26, 2009
FG syndrome, an X-linked multiple congenital anomaly syndrome: the clinical phenotype and an algorithm for diagnostic testingRobin Dawn Clark, John M Graham, Michael J Friez, et al.
American Journal of Medical Genetics|December 31, 1997
Evaluation of mental retardation: recommendations of a Consensus Conference: American College of Medical GeneticsC J Curry, R E Stevenson, D Aughton, et al.
American Journal of Medical Genetics. Part A|November 1, 2008
Behavior of 10 patients with FG syndrome (Opitz-Kaveggia syndrome) and the p.R961W mutation in the MED12 geneJohn M Graham, Jeannie Visootsak, Elisabeth Dykens, et al.
Nature Genetics|March 6, 2007
A recurrent mutation in MED12 leading to R961W causes Opitz-Kaveggia syndromeHiba Risheg, John M Graham, Robin D Clark, et al.
The Pediatric Infectious Disease Journal|December 17, 2011
Pneumococcal carriage and antibiotic resistance in young children before 13-valent conjugate vaccinePeter C Wroe, Grace M Lee, Jonathan A Finkelstein, et al.
Bone Marrow Transplantation|January 25, 2011
(90)Y-ibritumomab tiuxetan followed by reduced-intensity conditioning and allo-SCT in patients with advanced follicular lymphomaK E Abou-Nassar, K E Stevenson, J H Antin, et al.
American Journal of Human Genetics|May 13, 2005
Allan-Herndon-Dudley syndrome and the monocarboxylate transporter 8 (MCT8) geneCharles E Schwartz, Melanie M May, Nancy J Carpenter, et al.
Blood Advances|May 14, 2021
Low-cost transcriptional diagnostic to accurately categorize lymphomas in low- and middle-income countriesFabiola Valvert, Oscar Silva, Elizabeth Solórzano-Ortiz, et al.
MMWR. CDC Surveillance Summaries : Morbidity and Mortality Weekly Report. CDC Surveillance Summaries|August 25, 1995
Surveillance for anencephaly and spina bifida and the impact of prenatal diagnosis--United States, 1985-1994J D Cragan, H E Roberts, L D Edmonds, et al.
Leukemia|April 12, 2022
JAK3 mutations and mitochondrial apoptosis resistance in T-cell acute lymphoblastic leukemiaKimberly Bodaar, Natsuko Yamagata, Anais Barthe, et al.
Pageof 55

Showing results (441-450 of 550) with videos related to

Sort By:
Pageof 55
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 26, 2009
FG syndrome, an X-linked multiple congenital anomaly syndrome: the clinical phenotype and an algorithm for diagnostic testingRobin Dawn Clark, John M Graham, Michael J Friez, et al.
American Journal of Medical Genetics|December 31, 1997
Evaluation of mental retardation: recommendations of a Consensus Conference: American College of Medical GeneticsC J Curry, R E Stevenson, D Aughton, et al.
American Journal of Medical Genetics. Part A|November 1, 2008
Behavior of 10 patients with FG syndrome (Opitz-Kaveggia syndrome) and the p.R961W mutation in the MED12 geneJohn M Graham, Jeannie Visootsak, Elisabeth Dykens, et al.
Nature Genetics|March 6, 2007
A recurrent mutation in MED12 leading to R961W causes Opitz-Kaveggia syndromeHiba Risheg, John M Graham, Robin D Clark, et al.
The Pediatric Infectious Disease Journal|December 17, 2011
Pneumococcal carriage and antibiotic resistance in young children before 13-valent conjugate vaccinePeter C Wroe, Grace M Lee, Jonathan A Finkelstein, et al.
Bone Marrow Transplantation|January 25, 2011
(90)Y-ibritumomab tiuxetan followed by reduced-intensity conditioning and allo-SCT in patients with advanced follicular lymphomaK E Abou-Nassar, K E Stevenson, J H Antin, et al.
American Journal of Human Genetics|May 13, 2005
Allan-Herndon-Dudley syndrome and the monocarboxylate transporter 8 (MCT8) geneCharles E Schwartz, Melanie M May, Nancy J Carpenter, et al.
Blood Advances|May 14, 2021
Low-cost transcriptional diagnostic to accurately categorize lymphomas in low- and middle-income countriesFabiola Valvert, Oscar Silva, Elizabeth Solórzano-Ortiz, et al.
MMWR. CDC Surveillance Summaries : Morbidity and Mortality Weekly Report. CDC Surveillance Summaries|August 25, 1995
Surveillance for anencephaly and spina bifida and the impact of prenatal diagnosis--United States, 1985-1994J D Cragan, H E Roberts, L D Edmonds, et al.
Leukemia|April 12, 2022
JAK3 mutations and mitochondrial apoptosis resistance in T-cell acute lymphoblastic leukemiaKimberly Bodaar, Natsuko Yamagata, Anais Barthe, et al.
Pageof 55